Canonical Allele Identifier: CA3879678

Gene: LMBRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.69700858A>C , CM000668.2:g.69700858A>C	GRCh38
NC_000006.11:g.70410750A>C , CM000668.1:g.70410750A>C	GRCh37
NC_000006.10:g.70467471A>C	NCBI36
NG_016012.1:g.101300T>G
NG_016012.2:g.170759T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018368.4:c.1095T>G MANE Select	NP_060838.3:p.Leu365=
ENST00000649934.3:c.1095T>G MANE Select	ENSP00000497690.1:p.Leu365=
NM_001363722.1:c.876T>G	NP_001350651.1:p.Leu292=
NM_001363722.2:c.876T>G	NP_001350651.1:p.Leu292=
NM_001367271.1:c.876T>G	NP_001354200.1:p.Leu292=
NM_001367272.1:c.876T>G	NP_001354201.1:p.Leu292=
NM_018368.3:c.1095T>G	NP_060838.3:p.Leu365=
ENST00000370570.5:c.876T>G	ENSP00000359602.1:p.Leu292=
ENST00000370570.6:c.876T>G	ENSP00000359602.1:p.Leu292=
ENST00000370577.7:c.1095T>G	ENSP00000359609.3:p.Leu365=
ENST00000472827.1:c.1084-56T>G	ENSP00000433385.1:n.1084-56T>G
ENST00000472827.2:c.*260T>G	ENSP00000433385.2:n.*260T>G
ENST00000647650.1:c.*592T>G	ENSP00000497808.1:n.*592T>G
ENST00000647655.1:n.2698T>G
ENST00000647934.1:n.1415T>G
ENST00000647964.1:c.876T>G	ENSP00000496784.1:p.Leu292=
ENST00000648168.1:c.876T>G	ENSP00000498178.1:p.Leu292=
ENST00000648210.1:n.906T>G
ENST00000648265.1:n.962T>G
ENST00000648303.1:c.*668T>G	ENSP00000498133.1:n.*668T>G
ENST00000648394.1:c.876T>G	ENSP00000497302.1:p.Leu292=
ENST00000648635.1:c.*860T>G	ENSP00000497204.1:n.*860T>G
ENST00000648743.1:c.876T>G	ENSP00000497135.1:p.Leu292=
ENST00000649011.1:c.1161T>G	ENSP00000497575.1:p.Leu387=
ENST00000649028.1:c.876T>G	ENSP00000498034.1:p.Leu292=
ENST00000649054.1:c.*152T>G	ENSP00000496991.1:n.*152T>G
ENST00000649057.1:c.*660T>G	ENSP00000497639.1:n.*660T>G
ENST00000649166.1:c.*779T>G	ENSP00000496844.1:n.*779T>G
ENST00000649370.1:n.1286T>G
ENST00000649673.1:c.*451T>G	ENSP00000497864.1:n.*451T>G
ENST00000649679.1:c.876T>G	ENSP00000497387.1:p.Leu292=
ENST00000649744.1:n.1283T>G
ENST00000649795.1:c.*682T>G	ENSP00000498147.1:n.*682T>G
ENST00000649918.1:c.876T>G	ENSP00000497487.1:p.Leu292=
ENST00000649958.1:c.*680T>G	ENSP00000496827.1:n.*680T>G
ENST00000650035.1:c.876T>G	ENSP00000497703.1:p.Leu292=
ENST00000650043.1:n.1074T>G
ENST00000650107.1:c.876T>G	ENSP00000497124.1:p.Leu292=
ENST00000650124.1:c.*594-56T>G	ENSP00000497903.1:n.*594-56T>G
ENST00000650473.1:c.848T>G	ENSP00000497045.1:n.848T>G
XM_006715511.2:c.483T>G	XP_006715574.1:p.Leu161=
XM_011535941.1:c.876T>G	XP_011534243.1:p.Leu292=
XM_024446488.1:c.876T>G	XP_024302256.1:p.Leu292=